Peptide Medix product catalog

ET
Editorial Team
August 16, 2026 5 min read

KLOW, GLOW and Wolverine are not three strengths of the same product — they are three different component sets, and the milligram figure on the label describes total solid rather than anything about the ratio between components. Working out what is actually in a blend vial, and what that means analytically, is a short exercise in arithmetic that most descriptions skip.

What is in each

BlendComponentsCatalogue presentationNumber of distinct molecules
WolverineBPC-157 + TB-50010 mg (5/5) and 20 mg (10/10)2
GLOWBPC-157 + TB-500 + GHK-Cu70 mg total3
KLOWBPC-157 + TB-500 + GHK-Cu + KPV80 mg total4
Wolverine StackBPC-157, TB-500, GHK-Cu as three separate vials3-vial stack3, independently reconstituted

Wolverine is the simple case: a 1:1 co-formulation of the two most-studied tissue-repair peptides, catalogued as BPC-157 + TB-500. GLOW adds the copper tripeptide; KLOW adds KPV on top of that, and the K in the name is the KPV. The naming convention is essentially additive, which is why the total masses climb from 10–20 mg to 70 mg to 80 mg — most of that increase is the copper peptide, for reasons that are about molecular weight rather than emphasis.

Why the mass ratio misleads

The four component molecules span an unusually wide molecular-weight range for a single vial:

ComponentMolecular weightµmol per 10 mg
BPC-1571,419.55 Da≈ 7.0
TB-500 (heptapeptide)889.02 Da≈ 11.2
GHK-Cu403.93 Da≈ 24.8
KPV342.43 Da≈ 29.2

A GHK-Cu-heavy blend therefore contains far more molecules of copper peptide than the mass fraction suggests. Take a 70 mg GLOW vial composed of, say, 10 mg BPC-157, 10 mg TB-500 and 50 mg GHK-Cu: that is roughly 7.0 µmol, 11.2 µmol and 123.8 µmol respectively. By mass the copper peptide is about 71% of the vial; by molar quantity it is about 87% of the molecules present. Any interpretation framed in terms of receptor occupancy or signalling stoichiometry has to use the molar column, not the label.

The same applies to KPV — a tripeptide of 342.43 Da, the smallest molecule in the set, present in high molar quantity relative to its mass share. The general treatment of this arithmetic is in the reconstitution guide.

Reconstitution arithmetic for a blend

A blend has one volume and therefore one dilution factor applied to every component simultaneously — which is convenient and also the source of most confusion. Take an 80 mg KLOW vial reconstituted with 4 mL of solvent. The total solid concentration is 20 mg/mL, but no single component is at 20 mg/mL. If the vial were composed of 10 mg BPC-157, 10 mg TB-500, 50 mg GHK-Cu and 10 mg KPV, the reconstituted concentrations are 2.5, 2.5, 12.5 and 2.5 mg/mL respectively. In molar terms that is roughly 1.76 mM, 2.81 mM, 30.9 mM and 7.30 mM — a spread of more than seventeen-fold across components in the same solution.

Two habits keep this straight. Record concentrations per component rather than for the vial as a whole, and always carry the molar figure alongside the mass figure. A laboratory notebook entry that says "KLOW 20 mg/mL" is not a usable record; one that lists four components with their individual mass and molar concentrations is.

Chemical compatibility inside one vial

Co-formulating a copper complex with other peptides raises a legitimate compatibility question, and here the sequences answer it favourably. BPC-157 is Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val: no methionine, no cysteine, no tryptophan. TB-500 is Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln: same absences. KPV is Lys-Pro-Val: three residues, none of them oxidation-prone. The residues most vulnerable to copper-catalysed oxidation are simply not present in any of the partners, which is a genuinely good reason why this particular combination is chemically sensible rather than merely commercially convenient.

What does still apply is pH and chelation. The copper complex's stability depends on its coordination environment, so reconstitution solvent choice matters more for a copper-containing blend than for a plain peptide blend, and the blue colour of the reconstituted solution is a free indicator that the complex is intact.

Reading a multi-component certificate of analysis

This is where blends separate credible suppliers from careless ones. A single purity percentage for a four-component vial is not a meaningful statement — purity relative to what? A blend COA should show:

  1. A chromatogram in which every component resolves as its own peak, with retention times stated.
  2. An individual purity figure for each component, ideally with the method conditions that produced the separation.
  3. Mass-spectrometric identity confirmation for each component — four expected masses for KLOW, not one.
  4. A content or ratio assay stating how much of each component is present, not just that all are present.

The GHK-Cu peak is a useful sanity check here, because a copper complex behaves distinctly on reversed-phase chromatography and its expected mass of 403.93 Da is far from the others. If a blend COA shows a single peak or a single mass, it is describing something other than the vial in front of you. Method detail is in how to read a peptide COA.

Blend versus separate vials

The trade-off is straightforward. A blend fixes the ratio, uses one reconstitution volume and one set of arithmetic, and is convenient when the design calls for a fixed composition. Separate vials — the approach taken by the Wolverine Stack, which supplies three peptides as three independent vials — preserve the ability to vary one component while holding others constant, which is what any question about relative contribution actually requires.

In practice, replication work favours blends and mechanistic work favours separate vials. The broader argument is set out in peptide blends vs single vials, and the direct comparison of the two most-confused blends is in KLOW blend vs GLOW blend. The category sits in recovery blends.

The practical summary

Read a blend label as a statement of total solid, then immediately convert to molar quantities per component. Check the COA resolves and identifies every component individually. Note that the low-molecular-weight components dominate the molecule count regardless of what the mass fractions look like. And treat named blends as compositions to be verified rather than brands to be trusted — the names are catalogue conventions, and the chemistry is what you can actually check.

Frequently Asked Questions

What is the difference between KLOW, GLOW and Wolverine?
Wolverine is a two-component blend of BPC-157 and TB-500. GLOW adds GHK-Cu to those two. KLOW adds KPV to the GLOW combination, giving four components. The naming is additive, and the rising total masses mostly reflect the copper peptide's low molecular weight rather than any statement about emphasis.
Why does a blend contain so much more GHK-Cu by mass?
Because GHK-Cu has a molecular weight of only 403.93 Da against 1,419.55 Da for BPC-157. To supply a comparable molar quantity of a small molecule you need proportionally less mass, and to supply the larger molar quantities typical of copper peptide work you need considerably more milligrams. Mass fractions and molar fractions diverge sharply.
Is it chemically safe to combine a copper peptide with other peptides in one vial?
In this particular combination the sequences are favourable. BPC-157, the TB-500 heptapeptide and KPV all lack methionine, cysteine and tryptophan, the residues most susceptible to copper-catalysed oxidation. The remaining considerations are pH and competing chelators, which affect the copper complex itself rather than its partners.
What should a four-component blend COA show?
Four resolved chromatographic peaks with stated retention times, an individual purity figure for each component, four mass-spectrometric identity confirmations, and a content assay giving the amount of each component present. A single aggregate purity number for a multi-component vial does not describe its contents.
When are separate vials better than a blend?
Whenever the research question involves the relative contribution of components. A fixed-ratio blend cannot answer whether an observed effect depends on one component, because none can be varied independently. Separate vials cost extra handling steps but preserve that experimental freedom.
How do I know the copper complex survived reconstitution?
Colour. An intact GHK-Cu complex gives a distinctly blue solution because of the coordinated copper(II) centre. A colourless or off-colour solution suggests the coordination environment has been disturbed, typically by pH or by a competing chelator in the reconstitution solvent.

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